BMRB Entry 15956
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PDB ID:
Entry in NMR Restraints Grid
Validation report in NRG-CING
Chem Shift validation: AVS_anomalous, AVS_full, LACS, SPARTA
BMRB Entry DOI: doi:10.13018/BMR15956
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Title: NMR structure analysis of a BMP receptor PubMed: 18937504
Deposition date: 2008-09-17 Original release date: 2009-02-10
Authors: Klages, Jochen; Kotzsch, Alexander; Mueller, Thomas; Kessler, Horst
Citation: Klages, Jochen; Kotzsch, Alexander; Coles, Murray; Nickel, Joachim; Mueller, Thomas; Kessler, Horst. "The solution structure of BMPR-IA reveals a local disorder-to-order transition upon BMP-2 binding" Biochemistry 47, 11930-11939 (2008).
Assembly members:
Bone_Morphogenetic_Protein_Receptor_Type_IA, polymer, 102 residues, 11278.752 Da.
Natural source: Common Name: Human Taxonomy ID: 9606 Superkingdom: Eukaryota Kingdom: Metazoa Genus/species: Homo sapiens
Experimental source: Production method: recombinant technology Host organism: Escherichia coli
Entity Sequences (FASTA):
Bone_Morphogenetic_Protein_Receptor_Type_IA: GPEDTLPFLKCYCSGHCPDD
AINNTCITNGHCFAIIEEDD
QGETTLASGCMKYEGSDFQC
KDSPKAQLRRTIECCRTNLC
NQYLQPTLPPVVIGPFFDGS
IR
- assigned_chemical_shifts
Data type | Count |
13C chemical shifts | 379 |
15N chemical shifts | 101 |
1H chemical shifts | 626 |
Additional metadata:
Assembly:
Entity Assembly ID | Entity Name | Entity ID |
---|---|---|
1 | Bone Morphogenetic Protein Receptor Type IA | 1 |
Entities:
Entity 1, Bone Morphogenetic Protein Receptor Type IA 102 residues - 11278.752 Da.
27 N-terminal amino acids were truncated to facilitate structure analysis.
1 | GLY | PRO | GLU | ASP | THR | LEU | PRO | PHE | LEU | LYS | ||||
2 | CYS | TYR | CYS | SER | GLY | HIS | CYS | PRO | ASP | ASP | ||||
3 | ALA | ILE | ASN | ASN | THR | CYS | ILE | THR | ASN | GLY | ||||
4 | HIS | CYS | PHE | ALA | ILE | ILE | GLU | GLU | ASP | ASP | ||||
5 | GLN | GLY | GLU | THR | THR | LEU | ALA | SER | GLY | CYS | ||||
6 | MET | LYS | TYR | GLU | GLY | SER | ASP | PHE | GLN | CYS | ||||
7 | LYS | ASP | SER | PRO | LYS | ALA | GLN | LEU | ARG | ARG | ||||
8 | THR | ILE | GLU | CYS | CYS | ARG | THR | ASN | LEU | CYS | ||||
9 | ASN | GLN | TYR | LEU | GLN | PRO | THR | LEU | PRO | PRO | ||||
10 | VAL | VAL | ILE | GLY | PRO | PHE | PHE | ASP | GLY | SER | ||||
11 | ILE | ARG |
Samples:
sample_1: Bone Morphogenetic Protein Receptor Type IA, [U-99% 15N], 1.1 mM; H2O 95%; D2O 5%; potassium phosphate 10 mM; sodium azide 0.2 w/v
sample_2: Bone Morphogenetic Protein Receptor Type IA, [U-94% 13C; U-98% 15N], 0.5 mM; H2O 95%; D2O 5%; potassium phosphate 10 mM; sodium azide 0.2 w/v
sample_conditions_1: pH: 6.3; pressure: 1 atm; temperature: 298 K
Experiments:
Name | Sample | Sample state | Sample conditions |
---|---|---|---|
2D 1H-15N HSQC | sample_2 | isotropic | sample_conditions_1 |
2D 1H-13C HSQC | sample_2 | isotropic | sample_conditions_1 |
3D HNCO | sample_2 | isotropic | sample_conditions_1 |
3D HNCA | sample_2 | isotropic | sample_conditions_1 |
3D CBCA(CO)NH | sample_2 | isotropic | sample_conditions_1 |
3D HBHA(CO)NH | sample_2 | isotropic | sample_conditions_1 |
3D HNCACB | sample_2 | isotropic | sample_conditions_1 |
3D C(CO)NH | sample_2 | isotropic | sample_conditions_1 |
3D HCCH-TOCSY | sample_2 | isotropic | sample_conditions_1 |
3D HNHA | sample_1 | isotropic | sample_conditions_1 |
2D 1H-1H NOESY | sample_2 | isotropic | sample_conditions_1 |
3D 1H-15N NOESY | sample_2 | isotropic | sample_conditions_1 |
3D 1H-13C NOESY | sample_2 | isotropic | sample_conditions_1 |
3D HNHB | sample_1 | isotropic | sample_conditions_1 |
3D HCCH-COSY | sample_2 | isotropic | sample_conditions_1 |
3D 1H-15N-15N NOESY | sample_2 | isotropic | sample_conditions_1 |
3D 1H-15N-13C NIOESY | sample_2 | isotropic | sample_conditions_1 |
3D HCCH-TOCSY | sample_2 | isotropic | sample_conditions_1 |
3D HN(CA)HA | sample_2 | isotropic | sample_conditions_1 |
3D HN(CA)CO | sample_2 | isotropic | sample_conditions_1 |
Software:
X-PLOR NIH v2.9.4a, Schwieters, Kuszewski, Tjandra and Clore - structure solution
TOPSPIN v1.3, Bruker Biospin - collection, processing
SPARKY, Goddard - data analysis
TALOS, Cornilescu, Delaglio and Bax - data analysis
ProcheckNMR, Laskowski and MacArthur - geometry optimization
AQUA, Rullmann, Doreleijers and Kaptein - geometry optimization
WhatIF, Vriend - geometry optimization
NMR spectrometers:
- Bruker Avance 900 MHz
- Bruker DMX 750 MHz
- Bruker DMX 600 MHz
- Bruker DMX 600 MHz
Related Database Links:
PDB | |
DBJ | BAA03769 BAA04549 BAA07275 BAE20961 BAF84453 |
EMBL | CAA70474 CAA80257 CAA80678 |
GB | AAA21514 AAA21515 AAB33865 AAH28383 AAH42611 |
REF | NP_001070268 NP_001138622 NP_001191696 NP_001247522 NP_001267643 |
SP | P36894 P36895 Q78EA7 |
TPG | DAA14159 |
Download simulated HSQC data in one of the following formats:
CSV: Backbone
or all simulated shifts
SPARKY: Backbone
or all simulated shifts